Short‐ and long‐interval intracortical inhibition in EPM1 is related to genotype

OBJECTIVE: Progressive myoclonic epilepsy type 1 (EPM1) is caused by biallelic alterations in the CSTB gene, most commonly dodecamer repeat expansions. Although transcranial magnetic stimulation (TMS)–induced long‐interval intracortical inhibition (LICI) was previously reported to be normal in EPM1,...

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Detalles Bibliográficos
Autores principales: Silvennoinen, Katri, Säisänen, Laura, Hyppönen, Jelena, Rissanen, Saara M., Karjalainen, Pasi A., D'Ambrosio, Sasha, Jimenez‐Jimenez, Diego, Zagaglia, Sara, Rothwell, John C., Balestrini, Simona, Sisodiya, Sanjay M., Julkunen, Petro, Mervaala, Esa, Kälviäinen, Reetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107775/
https://www.ncbi.nlm.nih.gov/pubmed/36398398
http://dx.doi.org/10.1111/epi.17466

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107775/
https://www.ncbi.nlm.nih.gov/pubmed/36398398
http://dx.doi.org/10.1111/epi.17466

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